Synthesis of diphenyl sulfide from iodobenzene and thiophenol using Metal-Organic Framework Cu2(NDC)2(DABCO) as an efficient heterogeneous catalyst

Authors

  • Nguyen Van Chi Institute of Applied Science and Technology, Van Lang University, Vietnam Author
  • Dang Huynh Giao College of Engineering Technology, Can Tho University, Vietnam Author
  • Nguyen Thanh Tung Faculty of Chemical Engineering, Ho Chi Minh City University of Technology (HCMUT), Vietnam Author
  • Phan Nguyen Quynh Anh Faculty of Chemical Engineering, Ho Chi Minh City University of Technology (HCMUT), Vietnam Author
  • Phan Thanh Son Nam Faculty of Chemical Engineering, Ho Chi Minh City University of Technology (HCMUT), Vietnam. Vietnam National University Ho Chi Minh City, Vietnam. Author

DOI:

https://doi.org/10.51316/jca.2020.072

Keywords:

C-S coupling, iodobenzene, LiO-t-Bu, Cu2(NDC)2DABCO, thiophenol

Abstract

A metal-organic framework Cu2(NDC)2(DABCO) was synthesized from copper nitrate trihydrate, 2,6-Napthalenedicarboxylic acid (H2NDC), and 1,4-diazabicyclo[2.2.2]octane (DABCO) by solvothermal method. Its physicochemical properties were confirmed by several techniques such as X-ray powder diffraction (PXRD), Fourier transform infrared (FT-IR), scanning electron microscopy (SEM), and transmission electron microscopy (TEM). Cu2(NDC)2(DABCO) appeared as well-shaped crystals. To get diphenyl sulfide as desired product from the C-S cross coupling reaction of iodobenzene and thiophenol, the Cu2(NDC)2(DABCO) was used as heterogeneous catalyst  in the presence of LiO-tBu as base. The results showed that the transformation could proceed with more than 93% reaction conversion being obtained after 6 h at 120 oC when using 5 mol% Cu2(NDC)2(DABCO) catalyst in the presence of LiO-tBu. The solid catalyst could be recovered and reused five times without a significant degradation in catalytic activity. The coupling reaction could only proceed to achieve major product in the presence of the Cu2(NDC)2(DABCO catalyst.

Downloads

Download data is not yet available.

References

G. De Martino, M. C. Edler, G. La Regina, A. Coluccia, M. C. Barbera, D. Barrow, R. I. Nicholson, G. Chiosis, A. Brancale, E. Hamel, M. Artico, R. Silvestri, Journal of .Medicinal Chemistry 49 (2006) 947 – 954. https://doi.org/10.1021/jm050809s

J. Hassan, M. Sevignon, C. Gozzi, E. Schulz, M. Lemaire, Chemical Reviews 102 (2002) 1359-1470. https://doi.org/10.1021/cr000664r

A. Van Bierbeek, M. Gingras, Tetrahedron Letter 39 (1998) 6283 – 6286. https://doi.org/10.1016/S0040-4039(98)01327-6

K. Masanori, O. Toshimi, T. Masahiro, S. Hiroshi, M. Toshihiko, Bulletin of the Chemical Society of Japan 58 (1985) 3657-3658. https://doi.org/10.1246/bcsj.58.3657

C.-F. Lee, Y.-L. Liu, S. S. Badsara, Chemistry an Asian Journal 9(2014) 706-722. http://doi.org/10.1002/asia.201301500

A. Correa, M. Carril, C. Bolm, Angewandte International Edition Chemie 47 (2008) 2880-2883. https://doi.org/10.1002/anie.200705668

Y.-C. Wong, T. T. Jayanth, C. –H. Cheng, Organic Letters 8(2006) 5613-5616. https://doi.org/10.1021/ol062344l

Y. Zhang, K. C. Ngeow, J. Y. Ying, Organic Letters 9(2007) 3495-3498. https://doi.org/10.1021/ol071248x.

A. Sujatha, A. M. Thomas, A. P Thankachan, G. Anilkumar, 2015 (2014) 1-28. https://doi.org/10.3998/ark.5550190.p008.779

L. Rout, T. K. Sen, T. Punniyamurthy, , Angewandte International Edition Chemie 46(2007) 5583-5586. https://doi.org/10.1002/anie.200701282

M. Eddaoudi, D. B. Moler, H. Li, B. Chen, T. M. Reineke, M. O'keeffe and O. M. Yaghi, Accounts of Chemical Research 34 (2001) 319-330. https://doi.org/10.1021/ar000034b

A. M. Shultz, O. K. Farha, J. T. Hupp and S. T. Nguyen, Journal of the American Chemical Society 131 (2009) 4204-4205. https://doi.org/10.1021/ja900203f

L. Zhu, X. Q. Liu, H. L. Jiang, and L. B. Sun, Chemical Reviews 117 (2017) 8129-8176. https://doi.org/10.1021/acs.chemrev.7b00091

A. Dhakshinamoorthy, A. M. Asiri, H. Garcia, Chemical Society Reviews 44 (2015) 1922-1947. https://doi.org/10.1039/C4CS00254G

R. Heck, O. Shekhah, O. Zybaylo, P. G. Weidler, F. Friedrich, R. Maul, W. Wenzel, C. Wӧll, Polymers. 3 (2011) 1565-1574. https://doi.org/10.3390/polym3031565

I. Luz, F.X. Llabrés i Xamena, A. Corma, Journal of Catalysis 276 (2010) 134-140. https://doi.org/10.1016/j.jcat.2010.09.010

N. T. S. Phan, C. W. Jones, Journal of Molecular Catalysis A: Chemical 253 (2006) 123-131. https://doi.org/10.1016/j.molcata.2006.03.019

Published

31-12-2020

Issue

Section

Full Articles

How to Cite

Synthesis of diphenyl sulfide from iodobenzene and thiophenol using Metal-Organic Framework Cu2(NDC)2(DABCO) as an efficient heterogeneous catalyst. (2020). Vietnam Journal of Catalysis and Adsorption, 9(4), 70-76. https://doi.org/10.51316/jca.2020.072

Share

Most read articles by the same author(s)

Similar Articles

1-10 of 77

You may also start an advanced similarity search for this article.